Viola Patrizia, Vroobel Katherine M, Devaraj Anand, Jordan Simon, Ladas George, Dusmet Michael, Montero Angeles, Rice Alexandra, Wotherspoon Andrew C, Nicholson Andrew G
Department of Histopathology, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Department of Histopathology, Royal Marsden Foundation Trust, London, UK.
Histopathology. 2016 Nov;69(5):752-761. doi: 10.1111/his.12998. Epub 2016 Jul 8.
Follicular dendritic cell sarcoma is a rare tumour reported to occur occasionally in association with the hyaline-vascular type of Castleman's disease (HVCD). Most cases arise in lymph nodes, although extranodal presentation is described.
Clinical, radiological and histological characteristics, including diagnosis on pre-resection material, were assessed in seven intrathoracic cases from five males and two females with a median age of 38 years. Clinical symptoms were related to mass location, six cases presenting within central and/or posterior mediastinal compartments and one within the lungs. Positron emission tomography-computed tomography demonstrated marked fluoro-deoxy-glucose avidity and the prominent vessels traversing the lesions. Four of six cases (67%) were misdiagnosed initially. HVCD was present in three cases. Two cases with high mitotic rates recurred after resection. All were positive for at least one of the follicular dendritic cell markers (CD21, CD35 and CD23). Six of seven cases (86%) show cyclin D1 expression ranging from 5% to 90%.
Follicular dendritic cell sarcoma is often misdiagnosed on biopsy and pathologists need to be aware of the tumour to request the relevant immunohistochemistry, especially in masses presenting in the central/posterior mediastinum with high vascularity and standardized uptake values. Background HVCD appears more common than previously thought.
滤泡树突状细胞肉瘤是一种罕见肿瘤,据报道偶尔与透明血管型Castleman病(HVCD)相关。大多数病例发生于淋巴结,不过也有结外表现的描述。
对来自5名男性和2名女性的7例胸腔内病例进行了临床、放射学和组织学特征评估,包括术前材料诊断,中位年龄为38岁。临床症状与肿块位置有关,6例位于纵隔中部和/或后部,1例位于肺内。正电子发射断层扫描-计算机断层扫描显示明显的氟脱氧葡萄糖摄取及贯穿病变的显著血管。6例中的4例(67%)最初被误诊。3例存在HVCD。2例有高有丝分裂率的病例术后复发。所有病例至少对一种滤泡树突状细胞标志物(CD21、CD35和CD23)呈阳性。7例中的6例(86%)显示细胞周期蛋白D1表达,范围为5%至90%。
滤泡树突状细胞肉瘤在活检时常被误诊,病理学家需要了解该肿瘤以便要求进行相关免疫组织化学检查,尤其是对于位于纵隔中部/后部、血管丰富且标准化摄取值高的肿块。背景HVCD似乎比之前认为的更常见。